美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA202306"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
10135-823-32 10135-823 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20250801 N/A ANDA ANDA202306 Marlex Pharmaceuticals, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-32)
10135-823-33 10135-823 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20250801 N/A ANDA ANDA202306 Marlex Pharmaceuticals, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 360 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-33)
10135-823-60 10135-823 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20250801 N/A ANDA ANDA202306 Marlex Pharmaceuticals, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-60)
10135-823-62 10135-823 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20250801 N/A ANDA ANDA202306 Marlex Pharmaceuticals, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-62)
10135-823-90 10135-823 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20250801 N/A ANDA ANDA202306 Marlex Pharmaceuticals, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-90)
10135-824-05 10135-824 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20250801 N/A ANDA ANDA202306 Marlex Pharmaceuticals, Inc. METFORMIN HYDROCHLORIDE 750 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-824-05)
10135-823-30 10135-823 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20250801 N/A ANDA ANDA202306 Marlex Pharmaceuticals, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-30)
10135-823-10 10135-823 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20250801 N/A ANDA ANDA202306 Marlex Pharmaceuticals, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-10)
10135-823-05 10135-823 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20250801 N/A ANDA ANDA202306 Marlex Pharmaceuticals, Inc. METFORMIN HYDROCHLORIDE 500 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-823-05)
10135-824-10 10135-824 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20250801 N/A ANDA ANDA202306 Marlex Pharmaceuticals, Inc. METFORMIN HYDROCHLORIDE 750 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-824-10)
10135-824-90 10135-824 HUMAN PRESCRIPTION DRUG METFORMIN HYDROCHLORIDE METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20250801 N/A ANDA ANDA202306 Marlex Pharmaceuticals, Inc. METFORMIN HYDROCHLORIDE 750 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (10135-824-90)
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